Canonical Allele Identifier: CA357430823

Gene: ADAMTS3

Linked Data

• dbSNP Id: rs1719309764
• MyVariant Identifiers: chr4:g.73179457C>G (hg19) ; chr4:g.72313740C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313740C>G , CM000666.2:g.72313740C>G	GRCh38
NC_000004.11:g.73179457C>G , CM000666.1:g.73179457C>G	GRCh37
NC_000004.10:g.73398321C>G	NCBI36
NG_046955.1:g.260060G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000286657.10:c.1682G>C MANE Select	ENSP00000286657.4:p.Gly561Ala
ENST00000286657.8:c.1682G>C	ENSP00000286657.4:p.Gly561Ala
ENST00000622135.1:c.1682G>C	ENSP00000480055.1:p.Gly561Ala
NM_014243.2:c.1682G>C	NP_055058.2:p.Gly561Ala
XM_011532421.1:c.1625G>C	XP_011530723.1:p.Gly542Ala
XM_011532422.1:c.1598G>C	XP_011530724.1:p.Gly533Ala
XM_011532423.1:c.1040G>C	XP_011530725.1:p.Gly347Ala
XM_011532424.1:c.950G>C	XP_011530726.1:p.Gly317Ala
XM_011532421.2:c.1625G>C	XP_011530723.1:p.Gly542Ala
XM_011532422.3:c.1598G>C	XP_011530724.1:p.Gly533Ala
NM_014243.3:c.1682G>C MANE Select	NP_055058.2:p.Gly561Ala